4201 - 4210 of 8620 Results
Title
Year
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OPENTitle: PINK1 phosphorylates ubiquitin predominantly in astrocytesJournal Name: npj Parkinson's DiseasePublisher: Springer Science and Business Media LLCVol: 5Issue #: 1Start Page:End Page:Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1038/s41531-019-0101-9Best OA location URL: https://www.nature.com/articles/s41531-019-0101-9.pdfCitation Count: 40
- Interactions between vascular burden and amyloid-β pathology on trajectories of tau accumulation2023OPENTitle: Interactions between vascular burden and amyloid-β pathology on trajectories of tau accumulationJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 3Start Page: 949End Page: 960Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awad317Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awad317/51665840/awad317.pdfCitation Count: 29
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OPENTitle: Machine learning nominates the inositol pathway and novel genes in Parkinson’s diseaseJournal Name: BrainPublisher: Oxford University Press (OUP)Vol: 147Issue #: 3Start Page: 887End Page: 899Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.1093/brain/awad345Best OA location URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awad345/51927901/awad345.pdfCitation Count: 18
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RESTRICTEDTitle: Clinical and imaging markers in premotor LRRK2 G2019S mutation carriersJournal Name: Parkinsonism & Related DisordersPublisher: Elsevier BVVol: 21Issue #: 10Start Page: 1170End Page: 1176Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1016/j.parkreldis.2015.08.007Citation Count: 37
- Mitochondrial clearance and maturation of autophagosomes are compromised in LRRK2 G2019S familial Parkinson’s disease patient fibroblasts2019OPENTitle: Mitochondrial clearance and maturation of autophagosomes are compromised in LRRK2 G2019S familial Parkinson’s disease patient fibroblastsJournal Name: Human Molecular GeneticsPublisher: Oxford University Press (OUP)Vol: 28Issue #: 19Start Page: 3232End Page: 3243Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1093/hmg/ddz126Citation Count: 59
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RESTRICTEDTitle: Divalent metal ions control activity and inhibition of protein kinasesJournal Name: MetallomicsPublisher: Oxford University Press (OUP)Vol: 9Issue #: 11Start Page: 1576End Page: 1584Publication Date:Open Access(OA) Status: RESTRICTEDLicense:DOI - Digital Object Identifier: 10.1039/c7mt00204aCitation Count: 52
- Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson’s disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004)2022OPENTitle: Generation of two human induced pluripotent stem cell lines from fibroblasts of Parkinson’s disease patients carrying the ILE368ASN mutation in PINK1 (LCSBi002) and the R275W mutation in Parkin (LCSBI004)Journal Name: Stem Cell ResearchPublisher: Elsevier BVVol: 61Issue #:Start Page: 102765End Page: 102765Publication Date:Open Access(OA) Status: OPENLicense: cc-by-nc-ndDOI - Digital Object Identifier: 10.1016/j.scr.2022.102765Best OA location URL: https://doi.org/10.1016/j.scr.2022.102765Citation Count: 3
- Unique Astrocyte Cytoskeletal and Nuclear Morphology in a Three-Dimensional Tissue-Engineered Rostral Migratory Stream2022OPENTitle: Unique Astrocyte Cytoskeletal and Nuclear Morphology in a Three-Dimensional Tissue-Engineered Rostral Migratory StreamJournal Name: NeurogliaPublisher: MDPI AGVol: 3Issue #: 1Start Page: 41End Page: 60Publication Date:Open Access(OA) Status: OPENLicense: cc-byDOI - Digital Object Identifier: 10.3390/neuroglia3010003Best OA location URL: https://www.mdpi.com/2571-6980/3/1/3/pdf?version=1646557010Citation Count: 4
- Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar Disorders2023OPENTitle: Genetic Investigation of Consanguineous Pakistani Families Segregating Rare Spinocerebellar DisordersJournal Name: GenesPublisher: MDPI AGVol: 14Issue #: 7Start Page: 1404End Page: 1404Publication Date:Open Access(OA) Status: OPENLicense: cc-by, cc-byDOI - Digital Object Identifier: 10.3390/genes14071404Best OA location URL: https://www.mdpi.com/2073-4425/14/7/1404/pdf?version=1688622677Citation Count: 8
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OPENTitle: Palliative Care and Parkinson's Disease: Time to Move Beyond CancerJournal Name: Movement DisordersPublisher: WileyVol: 36Issue #: 6Start Page: 1325End Page: 1329Publication Date:Open Access(OA) Status: OPENLicense:DOI - Digital Object Identifier: 10.1002/mds.28556Best OA location URL: https://www.ncbi.nlm.nih.gov/pmc/articles/8217287Citation Count: 21